Encapsulation composition for use with chewing gum and edible products

ABSTRACT

The present invention is method and composition for protecting an active ingredient and providing controlled release therefor, especially in a chewing gum composition, which includes a high molecular weight polyvinyl acetate blended with a hydrophobic plasticizer which forms a film with the high molecular weight polyvinyl acetate in the absence of an added solvent therefor. The active ingredient, such as the artificial sweetener aspartame, is blended into the encapsulating composition as, for example, by melt blend which can then be cooled to a solid and ground into particulate. The encapsulated active ingredient can then be used in a composition for ingestion by a human in the form of, for example, a chewing gum with extended shelf life and highly controlled release of the active ingredient.

BACKGROUND OF THE INVENTION

This is a divisional of copending application Ser. No. 816,769 filed onJan. 7, 1986.

The present invention relates to the art of providing protection foractive food ingredients, and, in particular, to protecting foodingredients by encapsulation.

It has been known in the art of food preparation to provide protectionfor different ingredients included in food compositions by means ofprotective coatings. Such protective systems have been employed forvarious reasons such as for protection of the active ingredient, bothwhile on the shelf and during use, and for prolonged release in the oralcavity and/or systemically. As used herein, "active ingredient" can bean ingredient such as a sweetener, soluble dietary fiber, a flavoringagent, a bio-effecting ingredient, such as a medicinal drug orpharmaceutical agent, and a breath-freshening ingredient.

Protective systems for active ingredients encounter unique problems whenused in chewing gum compositions since gum compositions include asoluble portion which is consumed during chewing and an insolublemasticatory portion which remains in the oral cavity as a cud or bolusthroughout chewing. The soluble portion is added by blending solublebulking agents, flavorants, natural and synthetic sweeteners, etc. tothe gum base usually in the presence of heat in order to effectuatemixing. Thus, a protective system for an active must be able towithstand the rigors of heat and shear forces. Furthermore, since thegum base includes basically insoluble ingredients such as resins,elastomers, etc., any protection for an active ingredient included inthe base would have to be compatible to a certain degree with suchcomponents. Depending on the effect desired, the protected activeingredient can be incorporated into the base and/or added with thesoluble components or added after compositing.

Dipeptide sweeteners such as L-aspartyl-L-phenyl-alanine methylester(aspartame), which have been widely recognized as an extremelygood-tasting non-caloric sweetener for use in a variety of foodproducts, have been found to be particularly troublesome, especially,when used in chewing gum products. Unfortunately, aspartame is extremelyunstable in the presence of moisture and undergoes hydrolyticdegradation and subsequent loss of sweetness. Elevated temperatures andspecific pH ranges may accelerate the hydrolytic degradation.Additionally, aspartame is known to react with a number of flavoringsand chemicals such as aldehydes and ketones. For example, aspartameloses its sweetness due to chemical reactions in the presence of flavoraldehyde-containing oils such as cinnamon. These flavor oils are used infood products and are popular in chewing gum and other confectioneryproducts. These compositions also generally contain moisture and may beexposed to elevated temperatures during their shelf life. The result isthe loss of aspartame and the corresponding loss of sweetnesscontributed thereby in the gum.

For example, U.S. Pat. No. 3,962,463 to Witzel discloses chewing gumcontaining on its surface tiny capsules of flavoring and/or flavorsfixed on an edible substrate which will release the flavor uponmastication. The flavoring ingredient can be micro-encapsulated ingelatin, waxes, polyethylene and the like, and printed on the surface ofthe gum as an aqueous slurry. The encapsulation can be effected in aconventional manner by blending liquid flavoring with a concentratedaqueous solution of gelating at a temperature below 25° C. whereby afine stable emulsion is formed. After treatment to impart moistureresistance, the emulsion can be spray dried while still cool to producea fine free-flowing powder each particle of which consists of a core offlavoring surrounded by a dry gelating wall. The gelatingmicro-encapsulated flavoring ingredient can be printed on the gum byeither direct or off-set Gravure printing. As can be seen, the provisionof a protection system according to the above-disclosure is a rathercomplex procedure which requires an additional manufacturing step inorder to be added to the gum product.

Other disclosures show the use of protective encapsulation of artificialsweeteners such as aspartame, saccharin, etc. For example, U.S. Pat.Nos. 4,122,195 and 4,139,639 disclose encapsulation of aspartame inCapsul dextrin and gum arabic. However, such encapsulants have beenfound to be of only limited effectiveness in preventing degradation ofmoisture sensitive aspartame since these encapsulants are hydrophilicand moisture-permeable.

U.S. Pat. No. 4,384,004 to Cea, et al. discloses preparation of anartificial sweetener, i.e., APM, in an encapsulated form with at leastone layer of a coating material selected from the group consisting ofcellulose, cellulose derivatives, starches, carbohydrates, gums,polyolefins, polyesters, waxes, vinyl polymers, gelatin, zein, andmixtures thereof in a ratio of coating material to APM which does notexceed 1:1. This coating material is applied to the APM while it is insolid particle form at temperatures below the decomposition temperatureof APM, e.g., up to about 200°, and preferably about 100° to 115° F. Theapplication of the Cea, et al. protective system requires a ratherelaborate energy-intensive coating procedure, e.g., fluidized bedcoating process, in which a strong upward stream or air current must beprovided. This results from, among other things, the requirement ofproviding the protective coating material in a solvent.

EPA 81110320.0, published June 16, 1982 (Publication No. 0053844), toAjinomoto Co., Inc., discloses a stabilized dipeptide-based sweeteningcomposition comprising (a) from 20 to 60% by weight of solid fat, (b)from 10 to 30% by weight emulsifier, (c) from 10 to 30% by weightpolysaccharide and (d) not more than 30% by weight of dipeptidesweetener. The compositions are prepared by heating the mixture of theingredients, cooling, and pulverizing to obtain powder of granules ofthe composition to obtain a ASTM mesh size of smaller than 12. Spraydrying the mixture is also disclosed.

U.S. Pat. No. 4,105,801 to Degliotti, discloses a confectionarycomprising a core portion and a shell adheringly enveloping the coreportion, whereby the shell is formed by an intimate mixture ofmicrocrystals of xylitol with a solid fatty substance in a proportion of0.5 to 15 parts by weight of fatty substance to each 100 parts by weightof xylitol. The fatty substance is preferably a mono-, di- ortriglyceride having a melting range of between 20° and 60° C.

While it would seem that hydrophobic encapsulating agent provide betterimpermeability and gradual release characteristics than hydrophiliccoatings, it is not known whether any hydrophobic coatings have beensuccessfully employed in the past for chewing gum ingredients. Mosthydrophobic materials which could be used as encapsulants, such as a lowmolecular weight polyvinyl acetate, waxes and fats, are dissolved in thechewing base when they are mixed into the heated gum mass during the gummanufacturing process.

Other hydrophobic materials such as high molecular weight polyvinylacetate and styrene butadiene rubber are substantially insoluble in foodgrade solvents which are required in encapsulating processes. However,U.S. Pat. No. 3,826,847 to Ogawa, et al. discloses encapsulation ofseasonings including sugar by use of high molecular eight polymers suchas high molecular weight polyvinyl acetate; e.g., having a degree ofpolymerization of 400. Ogawa, et al. describe combining the seasoning bydissolving the polyvinyl ester in a solvent such as ethanol, ethylacetate and the like to obtain a 2-30% by weight solution to which theseasoning is subsequently added with agitation in an amount at 1-20times the polyvinyl ester content to form a homogenous dispersion. Thena liquid which is miscible with the solution but immiscible with thepolyvinyl ester, such as ether, hexane, or the like, is slowly added tothe dispersion so that polyvinyl ester granules integrated with theseasoning are separated out in the form of non-adhesive particles forincorporation into chewing gum base. The particle size can be less than20 mesh, and preferably are less than 48 mesh. In order to produce theparticulate, however, several decantations are required as well as adrying procedure, such as energy-intensive suction.

Yet another protection protective system for encapsulation has beendisclosed in PCT/US 84,00108 including a shellac encapsulant, which ishydrophobic and insoluble in the gum base yet soluble in food-gradesolvents, to provide a substantially impermeable coating for activeingredients, such as aspartame. The method of encapsulation can beeffected by coating with a shellac-containing solution primarily by afluidized bed coating method wherein particles of the active ingredientare suspended in a stream of pressurized air and sprayed with a solutionof the encapsulating agent. The particles can also be coated in a rollerbed coating method wherein a suspension of the active agent and itssolvent is deposited on a heated, rotating drum, the solvent beingevaporated by the heat leaving coated ingredient particles which arescraped from the roller. In each of these methods, and, generally, allmethods of encapsulating which includes a solvent, an energy-intensivestep to drive off the solvent is required before use in the end foodproduct.

It is therefore, an object of the present invention to provide an activeingredient protection system which can be easily included in a foodcomposition such as a chewing gum composition without an additional stepin the manufacturing process.

Another object of the present invention is to provide an encapsulationsystem which is highly effective in preventing deterioration frommoisture.

A further object of the invention is to provide an encapsulation systemwhich can be applied without the use of a solvent system.

Still another object of the present invention is to provide anencapsulated active ingredient with a highly-controlled releasecharacteristic for use in a food product.

Yet another object of the present invention is to provide a protectivesystem for artificial sweeteners which deteriorate in the present ofmoisture for use in a chewing gum composition.

Another object of the invention is to provide a chewing gum compositionwith a highly-controlled active ingredient protection and releasesystem.

Other and further objects will become apparent to those skilled in theart in view of the disclosure set forth herein.

BRIEF DESCRIPTION OF THE INVENTION

The present invention includes in one aspect a chewing gum compositioncontaining an active ingredient encapsulated in a solvent freeencapsulation composition which includes a blend of a high molecularweight polyvinyl acetate and a hydrophic plasticizer, such blend capableof forming an encapsulating film in the absence of an added solvent. Thepolyvinyl acetate can have a molecular weight of from 20,000 MWU toabout 100,000 MWU, preferably from about 30,000 to about 60,000 MWU, andmost preferably about 40,000 MWU. The hydrophobic plasticizer comprisesa mono-, di-, or triglyceride, or ester derivative thereof, which have afatty acid chain of from about 16 to about 22 carbon atoms, andpreferably from about 18 to about 20 carbon atoms. The composition canbe made such that the ratio atoms. The composition can of the highmolecular weight polyvinyl acetate to hydrophobic plasticizer is fromabout 5:1 to about 1:5 and is preferably from about 2:1 to about 1:2.

The present invention also includes the encapsulated active ingredientwhich is protected from deterioration due to moisture and is providedwith controlled release for use in a product to be ingested by mammal,the active ingredient being selected from a group consisting of naturaland artificial sweeteners, soluble dietary fiber, flavoring agents andbio-effecting agents. The active ingredient can be encapsulated with theencapsulating composition by forming a film thereon in the absence of anadded solvent. The ratio of encapsulating composition to activeingredient can be from 1:1 to about 10:1, and is preferably from about3:1 to about 5:1, depending on the desired rate of release.

When the active component is a sweetener, it can be selected from solidnatural or synthetic dipeptide sweeteners, especially aspartame,glycyrrhizin, saccharin and its salts, acesulfame salts, cyclamates,steviosides, talin, dihydrochalcone compounds and mixtures thereof.

The active ingredient which is encapsulated can also be a flavoringagent such as spearmint oil, cinnamon oil, oil of wintergreen(methyl-salicylate), peppermint oil, citrus oil, fruit essences,cinnamyl acetate, cinnaldehyde, citral diethylacetal, dihydrocarvylacetate, eugenyl formate, p-methyl ambesol, food acids, and mixturesthereof, among others.

Dietary fibers as used herein means a component of food which isnon-digestible and non-metabolizable by humans. It is well known thatdietary fibers as they occur naturally in food sources also haveassociated with them a small digestible portion comprising fats,proteins, and carbohydrates. Dietary fiber can be divided into two broadcategories: insoluble dietary fibers and water-soluble dietary fibers.For purposes of this invention insoluble dietary fibers meansubstantially non-swellable dietary fibers. Soluble dietary fibers meandietary fiber which is water-soluble or water-swellable. Soluble dietaryfibers which can be encapsulated include but are not limited tonon-cellulosic polysaccharides, pectin, gums such as guar and locustbean, algal polysaccharides, cellulose, hemi-celluloses, lignin, as wellas mixtures thereof.

Finally, when the active ingredient is a bio-effecting agent, it can beselected from the group consisting of mineral supplements, analgesics,antipyretics, antiarrhythmics, ion exchange resins, appetitesuppressants, vitamins, anti-inflammatory substances, coronary dilators,cerebral dilators, peripheral vasodilators, anti-infectives,psychotropics, antimanics, stimulants, antihistamines, laxatives,decongestants, gastro-intestinal sedatives, antidiarrheal preparations,anti-anginal drugs, vasodilators, anti-hypertensive drugs,vasoconstrictors and migrane treatments, antibiotics, tranquilizers,antipsychotics, antitumor drugs, anticoagulants and antithromboticdrugs, hypnotics, sedatives, anti-emetics, anti-nauseants,anticonvulsants, neuromuscular drugs, hyper and hypoglycaemic agents,thyroid and antithyroid preparations, diuretics, antispasmodics, uterinerelaxants, nutritional additives, antiobesity drugs, anabolic drugs,erythropoietic drugs, antiasthmatics, expectorants, cough suppressants,mucolytics, anti-uricemic drugs and mixtures thereof.

The chewing gum composition of the present invention can also includeadditional other non-encapsulated sweeteners so that sequential releasecan be effected from the initial burst of flavor throughout a desiredtime period.

Once the active ingredient is mixed in a melt blend with theencapsulating agent, it can be cooled to a solid, e.g., at temperaturesof about 0° C. and then ground to a particulate for use in an ingestiblecomposition such as a food composition, which is in one example achewing gum. Alternatively the active ingredient can be encapsulated byspray congealing methods.

In one preferred embodiment the chewing gum composition of the inventionincludes artificial sweeteners such as saccharin and/or aspartame thatcan be protected from moisture deterioration and can be provided withthe controlled release by the encapsulating agent. This is especiallyeffective in use with aspartame which is moisture sensitive, and hasbeen found to increase the shelf life of an aspartame-containing chewinggum at a level well above 60% the original content of aspartame after 65weeks of shelf life.

According to one process of the present invention, the polyvinyl acetateand plasticizer, which can preferably be glyceryl monostearate, can beblended at a temperature from about 70° C. to about 90° C., andpreferably about 85° C., to which the active ingredient can be added andblended, followed by cooling to a solid and grinding to a particulate.

As a result of the present invention, a highly effective protectivecoating can be provided to an active ingredient in a food or a drugdelivery system, without the use of a solvent must be driven off inorder to encapsulate. Furthermore, the protective encapsulatingcomposition can be fine tuned to provide the high degree of control overthe release of the active agent, whether by masticatory forces incurredduring chewing or by dissolution systemically.

Other advantages of the present invention is that the encapsulatingsystem is noncariogenic, and the use of the present composition does notresult in cold flow of polyvinyl acetate during prolonged storage.

Moreover, glyceryl monostearate is used, it has the unexpected propertyof inhibiting the hydrolysis of polyvinyl acetate to acetic acid andpolyvinyl alcohol. Moreover, because of the hydrophobic nature of theencapsulating agent, artificial sweeteners subject to water hydrolysis,such as aspartame, are stabilized. The encapsulated artificialsweeteners can be used in any food or pharmaceutical application whereit is desirable to protect an artificial sweetener from moisture.

When used in a chewing gum composition, chewing gum sweeteners, bothnatural and artificial which are extracted from the chewing gum duringmastication, have a prolonged release which can be controlled bymanipulation of the formula used in the encapsulating composition.Consequently, sweetness perception can be extended for 10 to 20 minutes,which is a highly effective prolonged release agent. If encapsulatedflavor agent is included with the encapsulating agent, an extended longlasting sweetened flavor perception can also be achieved. Whenencapsulating aspartame, the moisture degradation usually occurring inchewing gum is stabilized and the gum retains its aspartame content overa long period of time while at the same time providing extendedsweetness perception in the gum.

For a better understanding of the present invention, together withfurther and other objects, reference is made to the followingdescription, taken in conjunction with the accompanying drawings, andits scope will be pointed out in the appended claims.

DETAILED DESCRIPTION OF THE INVENTION

Although the present invention includes a chewing gum composition havinga variety of encapsulated active ingredients and combinations thereof,it is particularly effective for providing protection for activeingredients which are sensitive to moisture and undergo degradation ordeterioration in the presence of a water environment. Furthermore, thepresent protective encapsulation system is very effective to provide ahighly controlled release of active ingredient from the gum composition.This has been found to be especially effective for the use withartificial sweeteners such as aspartame and saccharin, as well asflavoring agents, etc. which are incorporated into chewing gumcompositions, especially when the encapsulated active ingredient isincorporated during the production of the overall composition.

Accordingly, the present protective system includes a composition with afirst component of high molecular weight polyvinyl acetate, which can befrom 20,000 MWU, preferably 30,000 MWU to 60,000 MWU, and mostpreferably 40,000 MWU. The molecular weight units as used herein referto those determined by use of gel permeation chromotography, GPC. Highmolecular weight polyvinyl acetate, which has been found to be a uniquecomponent of the present invention, is a thermoplastic high polymer,having a highly crystalline structure, which makes it brittle. It isalso very inert as well as relatively insoluble in most solvents,especially water. Due to highly crystalline structure and the extremelybrittle texture of high molecular weight polyvinyl acetate it wouldusually not be considered useable in the role of an effectiveencapsulating composition which simultaneously protects from moisturedegradation while at the same time provides highly controllable releaseof the active ingredient.

However when the high molecular weight polyvinyl acetate is combinedwith the second component of the unique encapsulating composition ofpresent invention, which is a hydrophobic plasticizer capable of forminga film in combination with the high molecular weight polyvinyl acetateeven in the absence of a solvent therefor, the best qualities of thehigh molecular weight polyvinyl acetate can be taken advantage ofwithout the accompanying disadvantages related to structure and handlingproperties. It has been found that the plasticizer which is especiallyeffective in the unique encapsulating composition is a mono-, di- ortriglyceride having a melting point of from about 45° C. to about 70°C., which can be readily melt blended with the polyvinyl acetate toprovide the desired encapsulating agent even without the use of asolvent. The glyceride should be solid or semi-solid at room temperaturein order to be effective. The fatty acid components of the glyceridesused herein can have a carbon chain range of from 8 to 22 carbons, andit has been found that glyceryl monostearate is an especially effectiveplasticizer for polyvinyl acetate having a molecular weight of 40,000MWU.

When the unique hydrophobic plasticizers and high molecular weightpolyvinyl acetate are melt blended in a range of from about 70 to about90° C. according to the present invention, the usually difficult to coatartificial sweetener aspartame can be readily blended thereineffectively completely encapsulating each and every particle for latercooling and grinding into a particulate. Moreover when this compositionis provided as an encapsulant for aspartame, which is later incorporatedinto chewing gum, the resulting product has improved shelf stability andlonger lasting sweetness perception.

In addition to simple melting and blending, spray congealing methods arealso useful. These methods involve melting and blending the polyvinylacetate/plasticizer; dispersing the actives at high shear; and atomizingthe resultant dispersion or mixture into fine droplets, which solidifywhen they contact the cooler atmosphere.

Another unusual result is that the active ingredient encapsulated in thepolyvinyl acetate/glyceride composition can be added to a gumcomposition at temperatures comensurate with manufacturing processes sothat a separate manufacturing step is not required to effectincorporation into a gum product. This effect is unlike the resultsachieved with wax and gelatin encapsulants which would readily melt atsuch temperatures.

The term "glyceride" as used herein refers to glycerides which areesters of glycerol and fatty acids in which one or more of the hydroxylgroups of glycerol had been replaced by acid radicals. It appears thatthe gylceride component contributes to the flexibility and elasticity ofthe polyvinyl acetate, which as a blend, forms a film on the activeingredient core material, thus rendering the blend highly effective inits role as an encapsulant.

The encapsulating material can be prepared in a ratio of polyvinylacetate to glyceride in a ratio of from about 5:1 to about 1:5 andpreferably is between from about 2:1 to about 1:2 depending on the typeof release desired.

The active ingredient can be selected from a wide variety of materialssuch as sweeteners, soluble dietary fibers, flavoring agents, andbio-effecting agents such as medicaments and drugs. These materials canalso be used either singly or in combination.

The sweetener component may be selected from solid natural or syntheticsweeteners including amino acid based sweeteners, dipeptide sweetenerssuch as L-aspartyl-L-phenylalanine methylester (aspartame),glycyrrhizin, saccharin and its salts, acesulfame salts, cYclamates,steviosides, talin, dihydrocalcone compounds and mixtures thereof. Aparticularly effective combination of sweeteners has been found to beaspartame in combination with saccharin which can be prepared in theencapsulating composition in such a manner that they can be releasedover a period of time either simultaneously or sequentially. In fact,one of the primary advantages of the present inventions is that theencapsulated active ingredient can be composited such that its releaseis highly controlled by the amount of active ingredient with respect toencapsulating composition.

Flavoring agents useful in the present invention include synthetic solidflavoring agents and/or liquids derived from plants, leaves, flowers,fruits and so forth and combinations thereof. Representative flavoringliquids include: spearmint oil, cinnamon oil, oil of wintergreen(methylsalicylate) and peppermint oils. Also, artificial, natural orsynthetic fruit flavors such as citrus oil including lemon, orange,grape, lime and grapefruit and fruit essences including apple,strawberry, cherry, pineapple, can be used.

The amount of flavoring agent employed is normally a matter ofpreference subject to factors such as flavor type, base type andstrength. In general, amounts of 0.5% to about 3% by weight are used inchewing gum compositions with preferred amounts being from about 0.3% toabout 1.5% , the most preferred ranges being from 0.7 to about 1.2%.

The active ingredient can also be a bio-effecting agent such as a drugselected from the group consisting of mineral supplements, analgesics,antipyretics, antiarrhythmics, ion exchange resins, appetitesuppressants, vitamins, anti-inflammatory substances, coronary dilators,cerebral dilators, peripheral vasodilators, anti-infectives,psychotropics, antimanics, stimulants, antihistamines, laxatives,decongestants, gastro-intestinal sedatives, antidiarrheal preparations,anti-anginal drugs, vasodilators anti-hypertensive drugs,vasoconstrictors migrane treatments, antibiotics, tranquilizers,antipsychotics, antitumor drugs, anticoagulants and antithromboticdrugs, hypnotics, sedatives, anti-emetics, anti-nauseants,anticonvulsants, neuromuscular drugs, hyper and hypoglycaemic agents,thyroid and antithyroid preparations, diuretics, antispasmodics, uterinerelaxants, mineral and nutritional additives, antiobesity drugs,anabolic drugs, erythropoietic drugs, antiasthmatics, expectorants,cough suppressants, mucolytics, anti-uricemic drugs and mixturesthereof.

As previously explained, active ingredients which are sensitive tomoisture and subject to deterioration in the presence of moisture, willparticularly benefit from the present protective encapsulationcomposition and process since they can be protected for extended periodsof time. Furthermore, in the case of having a need to effect control-led release of a sweetener and bio-effecting agent, the presentinvention is very effective since release can be directly related tocomposition proportions. Thus, an active ingredient having, for example,a very bitter taste can be administered to an individual by simplyproviding a controlled release which is at such a low level that it doesnot reach the threshold of perception by the consumer. Likewise, drugscan be administered over a prolonged period of time by simply preparingan encapsulating composition which provides a low-level sustainedrelease. A further use is to provide sustained release of ahigh-intensity sweetener at a very low concentration such that evenwithout increasing the overall amount of sweetener, the perception bythe consumer of, for example, a gum composition can be sustained over aperiod of 10-20 minutes. When incorporating active ingredients into anyingestible composition, non-encapsulated active can also be included inorder to effect sequential release of the active to the consumer.

Encapsulated active ingredient can be prepared by blending theingredients preferably at an elevated temperature such as between 70° C.and 90° C. and adding thereto the active ingredient, followed by coolingthe thus formed well-blended active ingredient to a solid and grindingthe solid to a particulate, which can be subsequently included in thedelivery system. The cooled solid is usually ground sufficiently toenable the particulate to pass through a 30 mesh sieve.

If spray congealing methods for encapsulating are employed, a uniformspherical particle results. Uniformity in size and effectiveness of thecoating are also achieved using this method. Thus, the particle size ofthe spray-congealed encapsulated actives can be controlled by varyingthe nozzle size, pressure and temperature and grinding is not necessary.

The encapsulated active ingredient is capable of being added to a gumcomposition at elevated temperatures usually associated gum preparation,such as 45-55° C., and is capable of withstanding high shear associatedwith high-speed mixing, stirring or screw extruding.

SPECIFIC EXAMPLES OF THE INVENTION

The present examples relate to the preparation of encapsulatedartificial sweeteners, e.g., aspartame and saccharin formulation, whichwhen incorporated into chewing gums, provides improved shelf stabilityand longer lasting sweetness perception.

It is known that commercially available chewing gum products, generallycomprised of plasticizers, softeners, flavors and sweeteners, experiencea quick release of the sweeteners, e.g., in about 4-5 minutes, so thatsustained sweetness perception is lost. Furthermore, sugarless chewinggums exhibit a noticeably low initial sweetness perception and lack thepresent impact of sugar-containing gums. Artificial sweeteners such assaccharin and aspartame have been used to provide the strong initialsweetness impact, but due to rapid release of the sweeteners, thesweetness intensity decreases very rapidly. High concentrations ofsaccharin are not acceptable in that they lead to a bitter aftertaste ofsaccharin, whereas aspartame undergoes degradation during aging of thegum and also loses its sweetness. Thus, in one of the embodiments of thepresent invention, these problems can be avoided by the use ofencapsulated saccharin and/or aspartame in anhydrous gum.

The encapsulated saccharin can be released at a controlled ratethroughout the duration of chewing rather than in only the initial fewminutes, thus, reducing and even concealing its bitter aftertaste evenat high concentration. Furthermore, the encapsulated aspartame will notundergo degradation and lose its sweetness during aging in additionproviding a sustained release during chewing. Thus, by use of thepresent encapsulating composition prepared and coated on the artificialsweetener which are included in anhydrous gum, sustained sweetnessperception can be imparted to the chewing gum product while moisturedeterioration problems experienced by aspartame are significantlyreduced.

Examples have been prepared in accordance with the present invention toprovide anhydrous chewing gum having longer-lasting sweetness impact,these examples having compositions including chewable gum base, flavor,sweetener in an amount sufficient to impart normal accepted sweetness tothe gum, and an amount of encapsulated artificial sweetener includingsaccharin and L-aspartyl-L-phenylalanine methylester (APM) effective toproduce longer-lasting sweetness in the gum. The chewing gumcompositions can be either sugar-containing or sugarless with no extrawater present in either case. The saccharin and APM have beenencapsulated in a combination of high molecular weight polyvinyl acetateand glyceryl monostearate.

EXAMPLE 1

Encapsulated aspartame was prepared using 50 grams of polyvinyl acetateand 100 grams of glyceryl monostearate which were melted and mixed bymechanical stirring at a temperature of about 85° C. for about fiveminutes. After removing the melt blend from the heat, 40 grams of finelyground aspartame was added and blended into the molten mass thoroughlyfor an additional five minutes. The resulting semi-solid mass waschilled to obtain a solid, e.g., to 0° C., and ground sufficiently sothat the resulting particulate passed through a 30 mesh sieve. Thesample was subjected to APM analysis and found to contain 21% APM of thetotal weight, indicating negligible degradation or loss of APM duringthe preparation.

EXAMPLE 2

The process of Example 1 was repeated using 120 grams of polyvinylacetate and 62 grams of glyceryl mono- stearate in preparing the coatingmixture, to which 60 grams of saccharin were added in place of theaspartame shown in Example 1. Chemical analysis of the resultingparticulate indicated a free saccharin content of 24.6%, thus alsoindicating negligible loss during preparation.

EXAMPLES 3 and 4

Following the procedure of Example 1 the following compositions ofencapsulated aspartame and saccharin were also prepared.

    ______________________________________                                                             Parts by weight (g)                                                           Example No.                                              Ingredients            3       4                                              ______________________________________                                        Polyvinyl Acetate      20      35                                             Glyceryl Monostearate  30      15                                             APM                    5       --                                             Saccharin              --      5                                              % APM Found (total weight basis)                                                                     9.1     --                                             % APM Found (% of APM added)                                                                         100.0   --                                             % Saccharin Found (total weight basis)                                                               --      9.2                                            % Saccharin Found (% of saccharin added)                                                             --      100.0                                          ______________________________________                                    

EXAMPLES 5-9

Using the encapsulated artificial sweeteners made in Examples 1-4chewing gum product samples were made as shown in Table I:

                  TABLE I                                                         ______________________________________                                        Chewing Gum Compositions                                                                     Parts by Weight                                                Ingredients Control  Ex. 5  Ex. 6                                                                              Ext. 7                                                                              Ex. 8                                                                              Ex. 9                             ______________________________________                                        Gum Base    26.4     26.4   26.4 26.4  26.4 26.4                              Triacetin    1.3      1.3    1.5 --    --   --                                Vegetable Oil                                                                             --       --     --    1.7   1.5 --                                Sugar       70.6     69.1   --   --    69.5 --                                Sorbitol    --       --     70.3 68.0  --   68.2                              Peppermint Oil                                                                             1.2      1.2    1.2  1.2   1.2  1.2                              Ex. 1 Encapsu-                                                                            --        1.8   --   --    --   --                                lated APM                                                                     Ex. 2 Encapsu-                                                                            --       --      0.4 --    --   --                                lated SAC                                                                     Ex. 3 Encapsu-                                                                            --       --     --    2.6  --    2.6                              lated APM                                                                     Ex. 4 Encapu-                                                                             --       --     --   --     1.2 --                                lated SAC                                                                     Free APM Powder                                                                           0.3      --     --   --    --   --                                ______________________________________                                    

The above compositions were prepared by adding the sugar or sorbitol andencapsulated sweetener at approximately the same time under mechanicalstirring and in the absence of added heat for five minutes. The moltengum base along with the softener, previously melted at approximately 95°C., was transferred into the mixer and mixed for three minutes. Thefinished gum product was rolled and scored.

In order to evaluate the stability of encapsulated APM in chewing gumsas in Examples 5, 7 and 9, a contro batch with free APM was alsoprepared. These batches were subjected to observation at roomtemperature over a period of at least 50 weeks or more. The resultsobtained have been set forth below in Table II:

                  TABLE II                                                        ______________________________________                                        Stability of Encapsulated APM in Chewing Gum (20° C.)                  APM Level (ppm)                                                               Example Theoret-                                                              No.     ical     Initial 2 Wks 3 Wks 50 Wks                                                                              65 Wks                             ______________________________________                                        Control 3000     2750    1400  --     250  --                                 5       3750     3680    --    3450  2710  --                                 7       2340     2280    2290  --    --    1570                               9       2340     2260    2250  --    --    1560                               ______________________________________                                    

The results reported above clearly indicate a significantly superiorperformance of the product made by use of the present invention.

The chewing gums prepared in accordance with the invention have beenfound to retain discernible sweetness perception for as long as 30minutes of continuous chewing. Encapsulated APM, prepared in accordancewith the present invention, when incorporated to the anhydrous chewinggum formulation has been found to exhibit an excellent stability. Whenstored at 20° C. (room temperature) for 65 weeks, the gum products werefound to retain over 69% of their initial APM.

Furthermore, the chewing gums prepared in accordance with the inventionhave been found to retain discernible sweetness perception for as longas 30 minutes of continuous chewing.

Thus while there have been described what are presently believed to bethe preferred embodiments of the present invention, those skilled in theart will realize that other and further embodiments can be made withinthe true scope of the invention, and is intended to claim all suchchanges and modifications.

I claim:
 1. An edible solvent-free encapsulation composition for protecting against moisture comprising:a blend of high molecular weight polyvinyl acetate having a molecular weight of about 20,000 to about 100,000 MWU and a hydrophobic plasticizer, said polyvinyl acetate and hydrophobic plasticizer being present in a ratio of 5:1 to about 1:5 and wherein said blend is capable of forming an encapsulating film when mixed in a melt blend.
 2. The composition of claim 1 wherein the molecular weight of said polyvinyl acetate is from about 30,000 MWU to about 60,000 MWU.
 3. The composition of claim 1 wherein said hydrophobic plasticizer comprises a mono-, di- or triglyceride or ester derivatives thereof, said plasticizer having a fatty acid chain of from about 16 to about 20 carbon atoms.
 4. The composition of claim 1 wherein the ratio is from about 2:1 to about 1:2.
 5. The composition of claim 1 wherein said encapsulation is a film formed on an active ingredient.
 6. The composition of claim 5 wherein said active ingredient is selected from the group consisting soluble dietary fibers, bio-effecting agents, and mixtures thereof.
 7. An edible product comprising an encapsualted active ingredient which is protected from moisture deterioration and which exhibits controlled release, wherein said active ingredient is selected from the group consisting of soluble dietary fibers, bio-effecting agents, and mixtures thereof and said encapsulant is solvent-free and comprises a blend of high molecular weight polyvinyl acetate and a hydrophobic plasticizer in an edible matrix wherein the active ingredient and encapsulant are mixed in a melt blend.
 8. The product of claim 7 wherein said polyvinyl acetate has a molecular weight of from about 20,000 MWU to about 100,000 MWU and said hydrophobic plasticizer is selected from the group consisting of mono-, di- and triglycerides having a fatty acid chain length of from about 16 to about 22 carbon atoms.
 9. The product of claim 8 wherein said product is a confectionary product.
 10. The product of claim 8 wherein said product is a pharmaceutical product.
 11. The product of claim 7 wherein said soluble dietary fiber is selected from the group consisting of non-cellulosic polysaccharides, pectin, guar gum, locust bean gum, algal polysaccharides, cellulose, hemi-celluloses, lignin, and mixtures thereof.
 12. The product of claim 7 wherein said active ingredient is a bio-effecting agents selected from the group consisting of mineral supplements, analgesics, antipyretics, antiarrhythmics, ion exchange resins, appetite suppressants, vitamins, anti-inflammatory substances, coronary dilators, cerebral dilators, peripheral vasodilators, anti-infectives, psychotropics, antimanics, stimulants, antihistamines, laxatives, decongestants, gastrointestinal sedatives, antidiarrheal preparations, antianginal drugs, vasodilators, anti-hylpertensive drugs, vasoconstrictors and migrane treatments, antibiotics, tranquilizers, antipsychotics, antitumor drugs, anticoagulants and antithrombotic drugs, hypnotics, sedatives, anti-emetics, anti-nauseants, anticonvulsants, neuromuscular drugs, hyper and hypoglycaemic agents, thyroid and antithyroid preparations, diuretics, antispasmodics, uterine relaxants, nutritional additives, antiobesity drugs, anabolic drugs, erythropoietic drugs, antiasthmatics, expectorants, cough suppressants, mucolytics, anti-uricemic drugs and mixtures thereof. 